Neudle.com: orbicularis oculi muscle

Differential
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acetylcholine receptor antibody

adverse drug reaction

amyotrophic lateral sclerosis, differential diagnosis

anterior tibial muscle weakness

antistriational muscle antibody

cardiac arrest and resuscitation

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Coats syndrome

Collier's sign

congenital myopathy

creatine phosphokinase(CPK)elevated

descending paralysis

diplopia

distal muscle weakness

electromyogram, decremental response

eye closure

face, elongated

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

gag reflex, depressed

gait disorder

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, horizontal

gaze palsy, vertical

gene mutation

genetic neurologic disorders

genetic testing

hand weakness

histochemistry of muscle

hypophonia

hypotonia

immunohistochemistry

immunosuppressive agents

inclusion body myositis

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

leg weakness, bilateral

lid abnormalities

lid closure, weakness of

lid twitch

lordosis

mediastinum, mass of

Melkersson's syndrome

mestinon

misdiagnosis

mitochondrial disease

motor neuron disease

multicore myopathy

muscle atrophy, progressive

muscle biopsy

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic sneer

myopathy

myopathy, centronuclear

myopathy, inflammatory

myopathy, mitochondrial

nemaline rod myopathy

nerve conduction studies

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuroophthalmology

neurotoxin

nystagmus

ocular motility, disorders of

ocular myopathy

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

orbicularis oculi muscle

oropharyngeal weakness

overlap syndrome

penicillamine

percussion induced muscle contraction

progressive neurologic disorder

pseudointernuclear ophthalmoplegia

rapidly progressing neurologic illness

repetitive nerve stimulation

respiratory failure

review article

saccadic eye movements

saccadic eye movements, abnormal

scoliosis

seronegative

shoulder-girdle wasting

single-fiber electromyography

sleep

sloped shoulders

spinal muscular atrophy

standing difficulty

steroid

steroid therapy, CNS treatment and complications with

temporalis muscle wasting

tensilon

tensilon test, false negative

tensilon test, false positive

tensilon test, paradoxical

thymectomy

thymoma

tongue, weakness

toxins, nervous system

transverse smile

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

voice, abnormality of

walking, difficulty with

weakness

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight loss

wheelchair

whistle, inability to

winging of scapula

Showing articles 1650 to 1700 of 3180 << Previous Next >>

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Frequency and Prognosis of Stroke/TIA Among 4808 Survivors of Acute Myocardial Infarction
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Individual Risk Assessment for Intracranial Haemorrhage During Thrombolytic Therapy
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Evaluation Times for Patients with In-Hospital Strokes
Stroke 24:1817-1822, Alberts,M.J.,et al, 1993

Ischemic & Hemorrhagic Stroke in Pts on Oral Anticoagulants After Reconstruct for Chronic Lower Limb Ischemia
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Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
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Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
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Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
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Life-Threatening Organophosphate-Induced Delayed Polyneurop in Child After Accidental Chlorpyrifos Ingest
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Early Severe Infantile Botulism
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Sumatriptan and Chest Pain
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Transmural Myocardial Infarction with Sumatriptan
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Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Gastric Carcinoma Metastases to Extraocular Muscles
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Accelerated Neuropathy of Renal Failure
Arch Neurol 50:536-539, Ropper,A.H., 1993

Juvenile Myoclonic Epilepsy
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Guillain-Barre Syndrome (GBS) with Bilateral Optic Neuritis and Central White Matter Disease
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MRI of Guillain-Barre Syndrome
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Elevated Serum Levels of Tumor Necrosis Factor-a in Guillain-Barre Syndrome
Ann Neurol 33:591-596, 5631993., Sharief,M.K.,et al, 1993

Relapse in Guillain-Barre Syndrome after Treatment with Human Immune Globulin
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Human Immune Globulin Infusion in Guillain-Barre Syndrome:Worsening During & After Treatment
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Serologic Evidence of Previous Campylobacter Jejuni Infection in Patients with the Guillain-Barre Syndrome
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Fulminant Rhabdomyolysis in a Patient with Dermatomyositis
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Drug Therapy of Idiopathic Inflammatory Myopathies:Response to Prednisone Azathioprine, & Methotrexate
Am J Med 94:379-387, Joffe,M.M.,et al, 1993

The Treatment of Inclusion Body Myositis:A Retrospective Review & Random, Prospective Trial of Immunosupp Therapy
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
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Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
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Inclusion Body Myositis Presenting Solely as Dysphagia
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Acute Myopathy Associated with Large Parenteral Dose of Corticosteroid in Myasthenia Gravis
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Sudden Onset of Profound Weakness in a Toddler
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Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
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Antineuronal (anti-Ri) Antibodies in a Pt with Steroid-Responsive Opsoclonus-Myoclonus
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Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Psychogenic Myoclonus
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Klippel-Feil Syndrome:CT and MR of Acquired & Congen Abnormal of Cervical Spine & Cord
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Myopathy in the Elderly:Evaluation of the Histopathologic Spectrum and the Accuracy of Clinical Diagnosis
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Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
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Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
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The Natural History of Amyotrophic Lateral Sclerosis
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Clinicopath Conf
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Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
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Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
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Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
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Showing articles 1650 to 1700 of 3180 << Previous Next >>